Study on the Effectiveness and Safety of Luveltamab Tazevibulin Compared to Chemotherapy in Women with Relapsed Platinum-resistant Ovarian Cancer

1 1 1

What is this study about?

This clinical trial is focused on studying the effectiveness and safety of a new treatment called luveltamab tazevibulin (also known as STRO-002) for women with a type of cancer known as relapsed platinum-resistant epithelial ovarian cancer. This includes cancers that originate in the ovaries, fallopian tubes, or the lining of the abdomen, known as the peritoneum. The study will compare this new treatment to standard chemotherapy options chosen by the doctor, which may include medications like gemcitabine, paclitaxel, topotecan, or Caelyx (pegylated liposomal doxorubicin).

The purpose of the study is to evaluate how well luveltamab tazevibulin works compared to these standard treatments. Participants will receive either the new treatment or one of the standard chemotherapy options. The study will monitor the participants over a period of time to assess the treatment’s impact on the cancer and any side effects that may occur. The study will also use a special test called the VENTANA FOLR1 CDx Assay to identify patients who might benefit from the new treatment. This test checks for the presence of a protein called folate receptor alpha in the cancer cells.

Throughout the study, participants will receive their assigned treatment and undergo regular check-ups to monitor their health and the cancer’s response to the treatment. The study aims to provide valuable information on whether luveltamab tazevibulin can be a more effective option for treating this type of ovarian cancer compared to existing chemotherapy treatments. The study is expected to continue until 2027, with recruitment starting in 2024.

1 joining the study

Upon joining the study, eligibility is confirmed based on specific criteria, including age, type of cancer, and previous treatments.

A negative pregnancy test is required for participants of childbearing potential, and a commitment to avoid pregnancy during and after the study is necessary.

2 treatment assignment

Participants are assigned to receive either luveltamab tazevibulin or a chemotherapy treatment chosen by the investigator.

The chemotherapy options include gemcitabine, paclitaxel, topotecan, or pegylated liposomal doxorubicin.

3 treatment administration

The medications are administered through an infusion, which involves delivering the drug directly into the bloodstream over a set period.

The frequency and duration of the treatment depend on the specific medication and the treatment plan outlined by the healthcare provider.

4 monitoring and assessments

Regular monitoring is conducted to assess the effectiveness of the treatment and to check for any side effects.

This includes imaging tests to measure tumor response and blood tests to monitor overall health and organ function.

5 follow-up

After completing the treatment phase, follow-up visits are scheduled to continue monitoring health status and any long-term effects of the treatment.

Participants are encouraged to report any new symptoms or concerns during these visits.

Who Can Join the Study?

  • Must have high grade serous epithelial ovarian cancer, fallopian tube, or primary peritoneal cancer, confirmed by a pathology report.
  • Must be 18 years or older at the time of signing the consent form. If local laws require a higher age for adulthood, those laws apply.
  • Must have an ECOG performance status of 0 to 1, which means being fully active or having some symptoms but being able to carry out light work.
  • Must have a life expectancy of more than 3 months.
  • Must have a positive FOLR1 expression, which is a specific test result from a central laboratory.
  • Must have relapsed platinum-resistant epithelial ovarian cancer and have received 1 to 3 previous treatments. Specific conditions apply based on the number of treatments and response to them.
  • Must be considered suitable for treatment with certain chemotherapy drugs like gemcitabine, paclitaxel, topotecan, or PLD for platinum-resistant disease.
  • Must have had prior treatment with bevacizumab, unless there is a documented reason not to use it, such as certain medical conditions.
  • Must have at least one measurable lesion on a scan, as defined by specific medical guidelines.
  • Must have adequate bone marrow function, which means having enough healthy blood cells. Specific levels for different types of blood cells are required.
  • Must have adequate liver function, meaning certain liver enzymes and bilirubin levels must be within specified limits.
  • Must have adequate kidney function, with a creatinine clearance of at least 30 mL/min, which measures how well the kidneys are working.
  • Must have a serum albumin level of at least 2.5 g/dL, which is a protein in the blood.
  • Must have a QT interval on an ECG test that is less than 470 milliseconds, which is a measure of heart rhythm.
  • Must be able to comply with treatment and testing schedules.
  • If of childbearing potential, must have a negative pregnancy test and agree to use effective birth control or abstain from heterosexual intercourse during treatment and for at least 6 months after the last dose. Women not of childbearing potential include those who have had certain surgeries or are post-menopausal.

Who Cannot Join the Study?

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Istituto Oncologico Veneto Padua Italy
Mater Misericordiae University Hospital Dublin Ireland
Orszagos Onkologiai Intezet Budapest Hungary
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Centre hospitalier universitaire de Liege Liege Belgium
Universitair Ziekenhuis Gent Gent Belgium
Universitaetsklinikum Aachen AöR Aachen Germany
Az Maria Middelares Gent Gent Belgium
Istituto Tumori Bari Giovanni Paolo II Bari Italy
Fundacion Instituto Valenciano De Oncologia Valencia Spain
Centre Hospitalier Universitaire Dinant Godinne Sainte-Elisabeth-UCL-Namur Namur Belgium
Fakultni Nemocnice Bulovka Prague Czechia
Hospital Universitario Virgen De Las Nieves Granada Spain
Azienda Ospedaliera Ordine Mauriziano Di Torino Turin Italy
Caritas Traegergesellschaft Saarbruecken mbH (CTS) Saarbrücken Germany
Azienda Unita’ Locale Socio Sanitaria N. 2 Marca Trevigiana Treviso Italy
Hospital Universitario Ramon Y Cajal Madrid Spain
St James’s Hospital Dublin Ireland
University Of Debrecen Debrecen Hungary
Hospital Universitario Reina Sofía Cordoba Spain
Charite Universitaetsmedizin Berlin KöR Berlin Germany
Fakultni Nemocnice Brno Brno Czechia
University Hospital Galway Galway Ireland
Fakultni Nemocnice Kralovske Vinohrady Prague Czechia
Turku University Hospital Turku Finland
Universita’ Di Pisa Pisa Italy
Universidade De Santiago De Compostela Santiago De Compostela Spain
Alessandro Manzoni Hospital Lecco Italy
Hospital Son Llatzer Palma Spain
Rheinische Friedrich-Wilhelms-Universitaet Bonn Bonn Germany
Nemocnice AGEL Novy Jicin a.s. Novy Jicin Czechia
Hospital Universitario Virgen De Valme Sevilla Spain
Klinik Hietzing Vienna Austria
Vseobecna Fakultni Nemocnice V Praze Prague Czechia
Pirkanmaan hyvinvointialue Tampere Finland
Hospital Alvaro Cunqueiro Vigo Spain
Institut fuer Klinische Transfusionsmedizin und Immungenetik Ulm gGmbH Ulm Germany
Universita Degli Studi Di Brescia Brescia Italy
Servei De Salut De Les Illes Balears Palma Spain
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
University Hospital Ostrava Ostrava Czechia
Otto Von Guericke Universitaet Magdeburg Magdeburg Germany
Hwmixguam Mmzvfpwx Soanec Milan Italy
Ayjtjba Ogbmkgksiyh Ukkozimdcfouj Pccfb Parma Italy
Cszo Upydwlprtn Hbnoejhh Cork Ireland
Ibrnvtwa Cjngvg Dcclsnhqjxxqgbdch L'hospitalet De Llobregat Spain
Ijxzfflp Rpydzzyrq Pgo Lw Ssypxy Dmo Tfninm Dkhp Aomurys Izes Sittjs Meldola Italy
Althbkw Ozmkuargiij Pfu Lngctmypxjtzymiso Ctxdihqrpf Catania Italy
Hskymzrj Ucrqichiwm Cbfurmi Hdeastet Helsinki Finland
Ayahddo Ooshsmdrzhf Uiftvgywmjzyg Caeohjcscruo Dbxrs Sckreg E Dsvhb Svljfnz Dn Thshgl Turin Italy
Gvuhzayoggwqivvdv Vvylskntq Pjkl Aojozn Eixyavvc Ozmxme Kivrbj Gyor Hungary
Umyvjbuqkv Ol Aoukirq Edegem Belgium
Uziwawknku Dxysn Spggs Dp Rfgu Ld Sagcuxtq Rome Italy
Htcmhjyb Vdba dutlevkh Barcelona Spain

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
31.05.2024
Belgium Belgium
Not recruiting
31.05.2024
Czechia Czechia
Not recruiting
31.05.2024
Finland Finland
Not yet recruiting
31.05.2024
Germany Germany
Not recruiting
31.05.2024
Hungary Hungary
Not recruiting
31.05.2024
Ireland Ireland
Not recruiting
31.05.2024
Italy Italy
Not recruiting
31.05.2024
Spain Spain
Not recruiting
31.05.2024

Trial locations

Luveltamab Tazevibulin (STRO-002) is a medication being studied for its effectiveness and safety in treating women with relapsed platinum-resistant epithelial ovarian cancer. This type of cancer can also include cancers of the fallopian tube or primary peritoneal cancers. The medication targets cancer cells that express a specific protein called folate receptor alpha (FOLR1), which is often found in these types of cancers. The goal is to see if this medication can help control the cancer better than standard chemotherapy options.

Investigator’s Choice Chemotherapy refers to the standard chemotherapy treatments that doctors can choose from based on their experience and the specific needs of the patient. These treatments are commonly used to manage ovarian cancer that has not responded well to platinum-based chemotherapy. The study compares the effectiveness of these standard treatments with the new medication, Luveltamab Tazevibulin, to see which works better for patients.

Advanced Epithelial Ovarian Cancer – This is a type of cancer that begins in the cells on the surface of the ovary. It can also include cancers that originate in the fallopian tubes or the peritoneum, which is the lining of the abdominal cavity. The disease is characterized by the uncontrolled growth of abnormal cells that can spread to other parts of the body. As it progresses, it may cause symptoms such as abdominal bloating, pelvic pain, and changes in bowel habits. The cancer often spreads to nearby tissues and organs, making it more challenging to manage. It is typically diagnosed at an advanced stage due to the subtlety of early symptoms.

Trial ID:
2024-512477-27-00
Protocol code:
STRO-002-GM3
NCT ID:
NCT05870748
Trial Phase:
Therapeutic exploratory (Phase II)

Other Trials to Consider

  • A Phase I/II Study of GVV858 Alone or in Drug Combination for Patients with Advanced Hormone Receptor‑Positive, HER2‑Negative Breast Cancer

    Recruiting

    1 1 1
    Czechia Denmark France Germany Italy Spain
  • A study of EP0031 and drug combination for patients with advanced cancers having changes in the RET gene

    Recruiting

    1 1 1
    France Germany Italy Poland Spain